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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762470Generated: November 1, 2026

Phenol → Isoindoline

https://huagongshe.com/reaction/1762470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPropionic AcidHCID 1032—
Reactant2-TosylisoindolineHCID 259899—
SolventHydrogen BromideHCID 260—
ProductIsoindolineHCID 42247862.6%

Reaction Steps

A solution of 12.0 g (0.044 mol) of 2-(p-tolylsulfonyl) isoindoline, 12.0 g (0.13 mol) of phenol, 90 ml of 48% HBr, and 15 ml (0.201 mol) of propionic acid was refluxed for two hours. The mixture was cooled to room temperature, triturated with diethyl ether, and then added to a solution of 75 gm of sodium hydroxide in 200 ml of cold water. This mixture was extracted with diethyl ether and the combined ether extracts were washed with water. The organic phase was dried over magnesium sulfate, concentrated in vacuo and kugelrohr distilled to give 3.28 g (61%) of a white solid, m.p. 118°-127° C. NMR (CDCl3) δ 2.2 (1H,s), 4.0 (4H, s), 6.95 (4H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04833150
Source datasetuspto-grants-1989_05
ORD IDord-ed6003ffd0734e96b7db47a748fda2b7
Source noteuspto-grants-1989_05